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Sequences involved in accurate and efficient transcription of human c-myc genes microinjected into frog oocytes.

作者信息

Nishikura K

出版信息

Mol Cell Biol. 1986 Nov;6(11):4093-8. doi: 10.1128/mcb.6.11.4093-4098.1986.

DOI:10.1128/mcb.6.11.4093-4098.1986
PMID:3025632
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC367176/
Abstract

By microinjecting a series of deletion mutant constructs into Xenopus laevis oocytes, transcriptional control regions, two promoters, of the human c-myc gene were defined. In the case of the first promoter, sequences between -60 and -37 relative to the transcription start site contained an element essential for promoter activity. In the case of the second promoter, sequences between -66 and -56 relative to the initiation site appeared to be involved in accurate and efficient transcription. In both cases, the region identified as the essential promoter element contained GGGCGG or GGCGGG,GC box-like sequences, suggesting that c-myc gene promoter activity may be controlled by transcription factor Sp1 binding in the microinjected oocytes.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c4/367176/f877f914e098/molcellb00095-0539-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c4/367176/3f28bc727971/molcellb00095-0538-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c4/367176/bb8e13379988/molcellb00095-0539-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c4/367176/f877f914e098/molcellb00095-0539-b.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c4/367176/3f28bc727971/molcellb00095-0538-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c4/367176/bb8e13379988/molcellb00095-0539-a.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e8c4/367176/f877f914e098/molcellb00095-0539-b.jpg

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Sequences involved in accurate and efficient transcription of human c-myc genes microinjected into frog oocytes.
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Accurate and efficient transcription of human c-myc genes injected into Xenopus laevis oocytes.注射到非洲爪蟾卵母细胞中的人类c-myc基因的准确高效转录。
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Upstream domains of the Xenopus laevis rDNA promoter are revealed in microinjected oocytes.非洲爪蟾核糖体DNA启动子的上游结构域在显微注射的卵母细胞中被揭示。
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引用本文的文献

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Mol Cell Biol. 1997 Aug;17(8):4363-71. doi: 10.1128/MCB.17.8.4363.
2
Repeated CT elements bound by zinc finger proteins control the absolute and relative activities of the two principal human c-myc promoters.与锌指蛋白结合的重复CT元件控制着人类两个主要c-myc启动子的绝对活性和相对活性。
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Identification of two enhancer elements downstream of the human c-myc gene.

本文引用的文献

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RNA processing in microinjected Xenopus oocytes. Sequential addition of base modifications in the spliced transfer RNA.显微注射非洲爪蟾卵母细胞中的RNA加工。剪接转运RNA中碱基修饰的顺序添加。
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Cloning and characterization of a human c-myc promoter-binding protein.一种人类c-myc启动子结合蛋白的克隆与特性分析
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Role of E2F transcription factor in E1A-mediated trans activation of cellular genes.E2F转录因子在E1A介导的细胞基因反式激活中的作用。
J Virol. 1991 Jul;65(7):3547-52. doi: 10.1128/JVI.65.7.3547-3552.1991.
10
Sequences in the human c-myc P2 promoter affect the elongation and premature termination of transcripts initiated from the upstream P1 promoter.人类c-myc P2启动子中的序列会影响从上游P1启动子起始的转录本的延伸和提前终止。
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Cell-cycle control of c-myc but not c-ras expression is lost following chemical transformation.化学转化后,c-myc的细胞周期控制丧失,但c-ras的表达未受影响。
Cell. 1984 Feb;36(2):241-7. doi: 10.1016/0092-8674(84)90217-4.
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Regulation of myc gene expression in HL-60 leukaemia cells by a vitamin D metabolite.一种维生素D代谢物对HL-60白血病细胞中myc基因表达的调控
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